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LATE to the PART-y.
Josephs KA, Mackenzie I, Frosch MP, Bigio EH, Neumann M, Arai T, Dugger BN, Ghetti B, Grossman M, Hasegawa M, Herrup K, Holton J, Jellinger K, Lashley T, McAleese KE, Parisi JE, Revesz T, Saito Y, Vonsattel JP, Whitwell JL, Wisniewski T, Hu W. Josephs KA, et al. Among authors: hasegawa m. Brain. 2019 Sep 1;142(9):e47. doi: 10.1093/brain/awz224. Brain. 2019. PMID: 31359030 Free PMC article. No abstract available.
Unique tauopathy in Fukuyama-type congenital muscular dystrophy.
Saito Y, Motoyoshi Y, Kashima T, Izumiyama-Shimomura N, Toda T, Nakano I, Hasegawa M, Murayama S. Saito Y, et al. Among authors: hasegawa m. J Neuropathol Exp Neurol. 2005 Dec;64(12):1118-26. doi: 10.1097/01.jnen.0000190069.10633.c2. J Neuropathol Exp Neurol. 2005. PMID: 16319722
Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS.
Inukai Y, Nonaka T, Arai T, Yoshida M, Hashizume Y, Beach TG, Buratti E, Baralle FE, Akiyama H, Hisanaga S, Hasegawa M. Inukai Y, et al. Among authors: hasegawa m. FEBS Lett. 2008 Aug 20;582(19):2899-904. doi: 10.1016/j.febslet.2008.07.027. Epub 2008 Jul 24. FEBS Lett. 2008. PMID: 18656473 Free article.
Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies.
Arai T, Mackenzie IR, Hasegawa M, Nonoka T, Niizato K, Tsuchiya K, Iritani S, Onaya M, Akiyama H. Arai T, et al. Among authors: hasegawa m. Acta Neuropathol. 2009 Feb;117(2):125-36. doi: 10.1007/s00401-008-0480-1. Epub 2009 Jan 13. Acta Neuropathol. 2009. PMID: 19139911
[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].
Arai T, Hasegawa M, Nishihara M, Nonaka T, Kametani F, Yoshida M, Hashizume Y, Beach TG, Morita M, Nakano I, Oda T, Tsuchiya K, Akiyama H. Arai T, et al. Among authors: hasegawa m. Rinsho Shinkeigaku. 2008 Nov;48(11):990-3. doi: 10.5692/clinicalneurol.48.990. Rinsho Shinkeigaku. 2008. PMID: 19198141 Review. Japanese.
4,137 results